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CAS

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664972-42-3

2-(4-chlorophenyl)-7-phenylpyrazolo[1,5-a]pyrimidin-6-yl phenyl sulfone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 664972-42-3 Structure

  • Basic information

    1. Product Name: 2-(4-chlorophenyl)-7-phenylpyrazolo[1,5-a]pyrimidin-6-yl phenyl sulfone
    2. Synonyms: 2-(4-chlorophenyl)-7-phenylpyrazolo[1,5-a]pyrimidin-6-yl phenyl sulfone
    3. CAS NO:664972-42-3
    4. Molecular Formula: C24H16ClN3O2S
    5. Molecular Weight: 445.92074
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 664972-42-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-chlorophenyl)-7-phenylpyrazolo[1,5-a]pyrimidin-6-yl phenyl sulfone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-chlorophenyl)-7-phenylpyrazolo[1,5-a]pyrimidin-6-yl phenyl sulfone(664972-42-3)
    11. EPA Substance Registry System: 2-(4-chlorophenyl)-7-phenylpyrazolo[1,5-a]pyrimidin-6-yl phenyl sulfone(664972-42-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 664972-42-3(Hazardous Substances Data)

664972-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 664972-42-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,4,9,7 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 664972-42:
(8*6)+(7*6)+(6*4)+(5*9)+(4*7)+(3*2)+(2*4)+(1*2)=203
203 % 10 = 3
So 664972-42-3 is a valid CAS Registry Number.

664972-42-3Downstream Products

664972-42-3Relevant articles and documents

Single step synthesis of new fused pyrimidine derivatives and their evaluation as potent Aurora-A kinase inhibitors

Shaaban, Mohamed R.,Saleh, Tamer S.,Mayhoub, Abdelrahman S.,Farag, Ahmad M.

experimental part, p. 3690 - 3695 (2011/11/06)

A simple, facile, efficient and one pot three-component procedure for the synthesis of pyrazolo[1,5-a]pyrimidines, triazolo[1,5-a]pyrimidines and pyrimido[1,2-a]benzimidazoles ring systems incorporating phenylsulfonyl moiety was developed via the reaction

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